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Reprinted from FDA’s website by Guidance for Industry: Questions and Answers Regarding the Labeling of Dietary Supplements as Required by the Dietary Supplement and Nonprescription Drug Consumer
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Guidance for industry questions are a set of guidelines issued by regulatory authorities to provide clarity and recommendations for various industries on specific topics or regulations.
Any industry or organization that falls under the jurisdiction of regulatory authorities and operates within the covered scope of the specific guidance is required to file guidance for industry questions.
To fill out guidance for industry questions, the industry or organization needs to carefully review the provided guidance document, gather the necessary information, and follow the specific instructions mentioned in the document to complete the required sections or forms.
The purpose of guidance for industry questions is to provide clear guidelines and recommendations to industries, helping them understand and comply with regulatory requirements, ensuring the safety, quality, and effectiveness of products or services.
The specific information required to be reported on guidance for industry questions may vary depending on the topic or regulation being addressed. However, it typically includes details about the industry or organization, product or service being regulated, compliance measures, testing requirements, labeling instructions, and any other relevant information specified in the guidance document.
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